Canonical Allele Identifier: CA1538275
Gene: MYCN HGNC NCBI

Linked Data

dbSNP Id: rs755948961
gnomAD v2: 2-16085739-C-G
gnomAD v4: 2-15945617-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15945617C>G , CM000664.2:g.15945617C>G GRCh38
NC_000002.11:g.16085739C>G , CM000664.1:g.16085739C>G GRCh37
NC_000002.10:g.16003190C>G NCBI36
NG_007457.1:g.10057C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000703162.1:n.264C>G
ENST00000281043.4:c.915C>G MANE Select ENSP00000281043.3:p.Asn305Lys
ENST00000638417.1:c.282C>G ENSP00000491476.1:p.Asn94Lys
ENST00000281043.3:c.915C>G ENSP00000281043.3:p.Asn305Lys
NM_001293228.1:c.915C>G NP_001280157.1:p.Asn305Lys
NM_001293231.1:c.282C>G NP_001280160.1:p.Asn94Lys
NM_001293233.1:c.*850C>G NP_001280162.1:n.*850C>G
NM_005378.5:c.915C>G NP_005369.2:p.Asn305Lys
NM_005378.6:c.915C>G MANE Select NP_005369.2:p.Asn305Lys
NM_001293228.2:c.915C>G NP_001280157.1:p.Asn305Lys
NM_001293231.2:c.282C>G NP_001280160.1:p.Asn94Lys
NM_001293233.2:c.*850C>G NP_001280162.1:n.*850C>G